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Hydrochloric Acid → 3-Phenyl-2-benzamido-1-propanethiol

HRID 1856409
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HRID 1856409 반응식
[C:1]1([CH2:7][CH:8]([NH:11][C:12](=[O:19])[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:9]Cl)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.NC(N)=[S:22].[OH-].[Na+].Cl>C(O)C.O>[C:1]1([CH2:7][CH:8]([NH:11][C:12](=[O:19])[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:9][SH:22])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 209006N-(1-Chloro-3-phenylpropan-2-yl)benzenecarboximidic acidHCID 2723790Thiourea

생성물 1

HCID 233449073-Phenyl-2-benzamido-1-propanethiol

시약·촉매·용매 2

HCID 702Ethanol용매
HCID 962
Water
용매

실험 절차

80.4 millimole (mm) of 3-phenyl-2-benzamido-1-chloropropane and 80.4 mm of thiourea are dissolved in 300 ml of ethanol. The resulting solution is refluxed for three hours. 6.7 g of sodium hydroxide is dissolved in 40 ml of water and is added under an inert atmosphere to the solution which is thereafter refluxed for an additional 21/2 hours. The solution is then cooled and acidified to pH 1 with 1 N HCl. The resulting mixture is then poured over ice to yield a precipitate which is collected by filtration and then dissolved in chloroform. The chloroform is dried with magnesium sulfate and then evaporated to yield the solid 3-phenyl-2-benzamido-1-propanethiol.

후처리

  1. temperatureThe resulting solution is refluxed for three hours
  2. additionis added under an inert atmosphere to the solution which
  3. temperatureis thereafter refluxed for an additional 21/2 hours
  4. temperatureThe solution is then cooled
  5. additionThe resulting mixture is then poured over ice
  6. customto yield a precipitate which
  7. filtrationis collected by filtration
  8. dissolutiondissolved in chloroform
  9. dry with materialThe chloroform is dried with magnesium sulfate
  10. customevaporated

출처 및 근거

ORD 기록
ord-04a9c60c17ad4dd0a7e2682609dd8f0f
출처 데이터셋
uspto-grants-1980_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04219497

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